Job Description

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them.No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.

We are better together and together We Are Altasciences.

About the Role
As an Analytical Chemistry Scientist in the Dose Concentration Analysis (DCA) team, you will provide technical and scientific expertise in the required assay for method development, validation/qualification and execution of analytical projects in support of preclinical/clinical studies. This will require rigorous attention to detail, excellent communication skills and the ability to work effectively on interdisciplinary teams of study directors, quality assurance, and other departmental personnel. Bring your strong schedule and work management skills to perform contracted projects according to the timeline provided and excellent data analysis skills with the ability to critically review data for scientific/technical merit and accuracy. Excellent communication skills for interacting with clients and possible clients will be necessary. Finally, our scientists need the ability to understand and conduct work under appropriate regulatory requirements.

What You’ll do Here

• Perform all study work in compliance with GLP regulations and maintain all related documentation in accordance with SOPs, protocol, and analytical plans

• Accountable for planning and managing timeline of assigned studies

• Review analytical data to ensure accuracy, completeness, consistency and regulatory compliance

• Respond to client inquires as needed to assist in study and assay design

• Provide scientific guidance and participate in the validation/qualification of new and current methods that are used in support of preclinical/clinical studies

• Prepare and modify SOPs as needed

• Provide indirect or direct line support of laboratory staff as assigned

• Design and execute appropriate analytical methods; critically review data and write study reports

• Serve as responsible/contributing scientist/principal investigator on GLP studies and as scientific resource for junior staff, peers and study directors

• Interact with clients through execution of analytical studies and provide on-time communication

• Work with departmental management to sustain analytical businesses with good science and regulation compliance

• Maintain all related study work documentation in accordance with standard operating procedures (SOPs), study protocol, and analytical plans

• Prepare abstracts and posters for presentation at scientific conferences

What You’ll Need to Succeed

• BS/MS in a biological or pharmaceutical science or related field with 4+ years in a related field; PhD and 2+ years relevant post-graduate experience

• Experience with method development, execution, analysis and writing scientific reports required

• Analytical background required; GLP experience preferred

• Intermediate computer skills including Microsoft Office suite

• English proficiency required to read, write, review, interpret and summarize scientific material

• Effective communication to diverse groups: clients, vendors, internal and external colleagues

• Advanced maths skills as required for data analysis, interpretation and graphical presentation skills

• Remain current with state-of-the-art technology

• Remain current with regulatory guidance and industry standards related to analysis

• Multi-tasking and strong organizational and project management skills

• Experience with Empower software preferred

Work Authorization & Sponsorship

Applicants must be legally authorized to work in the United States. Altasciences is unable to provide sponsorship, sponsorship transfers, or visa maintenance for this position. All applicants must possess valid work authorization that does not require employer sponsorship now or in the future.

What We Offer

The pay range estimated for this position is $85,000 - $102,000 annually. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.

Benefits

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences’ Benefits Package Includes:

• Health/Dental/Vision Insurance Plans

• 401(k)/RRSP with Employer Match

• Paid Vacation and Holidays

• Paid Sick and Bereavement Leave

• Employee Assistance & Telehealth Programs

• Telework when applicable.

Altasciences’ Incentive Programs Include:

• Training & Development Programs

• Employee Referral Bonus Program

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MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH

Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!